510(k) K950264 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
MAGLIFE
| Applicant | Odam, North Attleboro MA, US |
| Decision | Substantially Equivalent, Sep 27, 1996 |
| Received | Jan 23, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950264
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.